Verify company and product information
Check the legal entity, product name, model and specification, intended use, and validity period item by item, and align the project configuration with formal attachments. Do not rely solely on summaries in promotional materials.
Maintain version records
Add dates and version numbers to technical materials, quotation configurations, and meeting notes so the review team works from the same information.
Include professional review points
Regulatory classification, installation conditions, and clinical-use boundaries should be reviewed by the appropriate qualified professionals. All content shown on this site is demonstration material.